ClinVar Miner

List of variants in gene FASTKD2 reported as likely benign by GeneDx

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Gene type:
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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_001136193.2(FASTKD2):c.1814-53G>A rs13390575 0.01339
NM_001136193.2(FASTKD2):c.991-68A>G rs13392746 0.01317
NM_001136193.2(FASTKD2):c.2013+168C>T rs115621342 0.01062
NM_001136193.2(FASTKD2):c.2013+281A>G rs114849970 0.00708
NM_001136193.2(FASTKD2):c.-50-77C>A rs140026989 0.00514
NM_001136193.2(FASTKD2):c.1899-280G>A rs147371880 0.00415
NM_001136193.2(FASTKD2):c.149A>G (p.Lys50Arg) rs141447598 0.00289
NM_001136193.2(FASTKD2):c.-30T>C rs145438423 0.00261
NM_001136193.2(FASTKD2):c.1114+30A>G rs146433757 0.00251
NM_001136193.2(FASTKD2):c.1594+21T>C rs200919016 0.00251
NM_001136193.2(FASTKD2):c.2018A>G (p.Asn673Ser) rs142211558 0.00196
NM_001136193.2(FASTKD2):c.1898+92C>T rs77690144 0.00088
NM_001136193.2(FASTKD2):c.1501G>A (p.Ala501Thr) rs368402276 0.00051
NM_001136193.2(FASTKD2):c.1389C>T (p.Tyr463=) rs200425724 0.00029
NM_001136193.2(FASTKD2):c.882-3C>T rs41272661 0.00026
NM_001136193.2(FASTKD2):c.756G>A (p.Gln252=) rs377619612 0.00019
NM_001136193.2(FASTKD2):c.1255-7T>C rs757255885 0.00014
NM_001136193.2(FASTKD2):c.1080T>C (p.Leu360=) rs376045225 0.00011
NM_001136193.2(FASTKD2):c.2124C>T (p.Ser708=) rs200616436 0.00007
NM_001136193.2(FASTKD2):c.1115-10A>G rs747618392 0.00006
NM_001136193.2(FASTKD2):c.1353A>G (p.Leu451=) rs369427864 0.00005
NM_001136193.2(FASTKD2):c.1295G>A (p.Arg432Gln) rs372022584 0.00004
NM_001136193.2(FASTKD2):c.748T>C (p.Leu250=) rs748570624 0.00003
NM_001136193.2(FASTKD2):c.1813+14T>C rs1057521261 0.00002
NM_001136193.2(FASTKD2):c.1255-16A>G rs757982614 0.00001
NM_001136193.2(FASTKD2):c.1395T>C (p.Ser465=) rs376370564 0.00001
NM_001136193.2(FASTKD2):c.1885A>G (p.Thr629Ala) rs754915967 0.00001
NM_001136193.2(FASTKD2):c.777+14G>A rs752997524 0.00001
NM_001136193.2(FASTKD2):c.1029G>A (p.Leu343=) rs1553596141
NM_001136193.2(FASTKD2):c.1427+20dup rs371981683
NM_001136193.2(FASTKD2):c.1595-12_1595-11del
NM_001136193.2(FASTKD2):c.1814-72_1814-71dup rs5838043
NM_001136193.2(FASTKD2):c.182T>C (p.Leu61Ser) rs863223960
NM_001136193.2(FASTKD2):c.2013+12dup rs34386348
NM_001136193.2(FASTKD2):c.2013+179C>G rs116779051
NM_001136193.2(FASTKD2):c.2014-12_2014-11del rs770341016
NM_001136193.2(FASTKD2):c.261T>A (p.Asp87Glu) rs863223961
NM_001136193.2(FASTKD2):c.66C>T (p.Gly22=) rs866874741
NM_001136193.2(FASTKD2):c.991-13G>C rs13421046

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